Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g26820 | A10 | 21108612 | C | T | missense_variant | MODERATE | c.2279G>A|p.Arg760Lys |
S259 |
2 | BAA10g26820 | A10 | 21108821 | G | A | synonymous_variant | LOW | c.2070C>T|p.Asn690Asn |
S138 |
3 | BAA10g26820 | A10 | 21109102 | C | T | missense_variant | MODERATE | c.1789G>A|p.Val597Ile |
S33 |
4 | BAA10g26820 | A10 | 21109252 | C | T | missense_variant | MODERATE | c.1639G>A|p.Glu547Lys |
S265 |
5 | BAA10g26820 | A10 | 21109262 | C | T | synonymous_variant | LOW | c.1629G>A|p.Lys543Lys |
S185 |
6 | BAA10g26820 | A10 | 21109357 | G | A | missense_variant | MODERATE | c.1534C>T|p.Leu512Phe |
S139 |
7 | BAA10g26820 | A10 | 21109462 | C | T | missense_variant | MODERATE | c.1429G>A|p.Asp477Asn |
S167 |
8 | BAA10g26820 | A10 | 21109985 | C | T | synonymous_variant | LOW | c.906G>A|p.Glu302Glu |
S10 |
9 | BAA10g26820 | A10 | 21110164 | G | A | stop_gained | HIGH | c.727C>T|p.Gln243* |
S103 |
10 | BAA10g26820 | A10 | 21110588 | G | A | synonymous_variant | LOW | c.303C>T|p.Phe101Phe |
S208 S219 |
11 | BAA10g26820 | A10 | 21110687 | G | A | synonymous_variant | LOW | c.204C>T|p.Leu68Leu |
S74 |